331,861 research outputs found

    Discorsi morali di Agostino Mascardi sù la tavola di Cebete Tebano.

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    Marca tip. en portSign.: *\p12\s, 2*\p6\s, A-Z\p12\s, 2A\p11\sPort. enmarcadaHoja de lám. calc.: "Per il Baba

    "Strilni kamen" s Baba lokve

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    The author analyzes the prehistoric stone axe-hammer found at the Baba lokva medieval settlement site in Kaštela (14th to 17th centuries), observing it from the aspect of mythological perception of such finds as apotropaic objects (amulets, talismans). Drawing numerous ethnological parallels in Croatia, Bosnia and other parts of Central Europe and archaeological parallels in northern Croatia (Ludbreg – Iovia, Paka fortification) and Dalmatia (Begovača – Biljane Donje), the author argues that the Baba lokva axe was used to protect dwellings from lightning or, perhaps, as a personal protection of its owner who carried it. It is a custom that has been preserved since the prehistoric pagan (proto-Slavic and proto-Indo-European) times, surviving to this day as part of traditional culture.Autor obrađuje nalaz prapovijesne kamene sjekire-čekića na srednjovjekovnom naseobinskom lokalitetu Baba lokva u Kaštelima (14. – 17. st.) s aspekta mitološkog poimanja takvih nalaza kao apotropejskih predmeta (amuleti, talismani). Pomoću brojnih etnoloških paralela u Hrvatskoj i Bosni, kao i u široj srednjoeuropskoj regiji, te arheoloških paralela u sjevernoj Hrvatskoj (Ludbreg – Iovia, utvrda Paka) i u Dalmaciji (Begovača – Biljane Donje) dokazuje da je sjekira s Baba lokve bila u funkciji zaštite nastambi od groma ili možda osobne zaštite vlasnika koji ju je nosio. Radi se o običaju koji je preživio kao sirvival iz poganskih prapovijesnih vremena (praslavenskih i praindoeuropskih) i zadržao se do naših dana kao dio tradicijske kulture

    Chinese literary works translated into Baba Malay: a bibliographical study

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    Analyses 68 unique titles of Baba translated works published between 1889 and 1950. The titles are held in the libraries of the University of Malaya (UM), Science University Malaysia (USM), National University of Malaysia (UKM), the Dewan Bahasa dan Pustaka (DBP), National University of Singapore (NUS), National Library of Singapore (NLS) and the British Library (BL). The results reveal three periods of active publication of Baba translated works. A total of 18 works were translated before World War I, followed by 10 just after the war, 39 titles were published before the break of the World War II and 1 was identified in 1950. There were 103 persons involved in the 68 translated works, some of whom are responsible for more than one title. The most prominent translators were Chan Kim Boon, Wan Boon Seng, Seow Chin San and Lee Seng Poh. Some of the translators were also be editors, illustrators or editors. There were 31 publishers and 21 printing presses involved, all were located in Singapore. The most active publishers were Wan Boon Seng, Kim Seck Chy Press and Nanyang Romanised Malay Book Co. The translated works mainly cover historical classical Chinese stories, chivalrous stories, romances, folklore and legends. The titles were priced between 10 cents to 2 dollars in Straits currency. The University of Malaya Library held the largest number of unique title (62) out of which 15 were unique titles

    Onconida tropis Baba & de Saint Laurent 1996

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    Onconida tropis Baba & de Saint Laurent, 1996 Onconida tropis Baba & de Saint Laurent, 1996: 491, figs 29, 34c. — Baba 2005: 299, 300. MATERIAL EXAMINED. — Tonga. BORDAU 2, stn CP 1526, 21°15.80’S, 174°59.20’W, 463-464 m, 2. VI.2000, 1 ♂ 6.1 mm (MNHN-Ga 5331). — Stn CP 1527, 21°16’S, 174°59’W, 483-509 m, 3. VI.2000, 1♂ 6.7 mm; 2 ovig. ♀♀ 5.7-6.7 mm; 1 ♀ 4.9 mm (MNHN-Ga 5332). — Stn CP 1538, 21°39’S, 175°19’W, 471-508 m, 4. VI.2000, 2 ♂♂ 5.9-6.7 mm (MNHN-Ga 5333). — Stn CP 1545, 21°17’S, 175°17’W, 444-447 m, 5. VI, 2000, 1 ♂ 4.9 mm; 3 ovig. ♀♀ 5.3-5.9 mm (MNHN-Ga 5334). — Stn CP 1552, 20°38’S, 174°58’W, 491-500 m, 6. VI.2000, 1 ♂ 4.6 mm (MNHN-Ga 5335). — Stn CP 1593, 19°06’S, 174°18’W, 436-442 m, 14. VI.2000, 1 ♀ 6.6 mm (MNHN-Ga 5336). — Stn CP 1643, 21°04.54’S, 175°22.50’W, 487 m, 22. VI.2000, 2 ♂♂ 4.2-5.2 mm; 3 ♀♀ 5.2-6.7 mm (MNHN-Ga 5337). SolomonIslands. SALOMON1,stnCP1831, 10°12.121’S, 161°19.236’E, 135-325 m, 5.X.2002, 25 ♂♂ 4.4-6.6 mm; 15 ovig. ♀♀ 5.0- 7.3 mm; 6 ♀♀ 5.5-6.8 mm (MNHN-Ga 5338). DISTRIBUTION. — Known from Indonesia (Kei Islands) and New Caledonia in 210- 480 m. The new occurrences extend the distribution range to the Solomon Islands and Tonga, in 135- 509 m. Genus Plesionida Baba & de Saint Laurent, 1996Published as part of Macpherson, Enrique & Baba, Keiji, 2006, New species and records of small galatheids (Crustacea, Decapoda, Galatheidae) from the Southwest and Central Pacific Ocean, pp. 443-456 in Zoosystema 28 (2) on page 455, DOI: 10.5281/zenodo.540290

    Plesionida psila Baba & de Saint Laurent 1996

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    Plesionida psila Baba & de Saint Laurent, 1996 Plesionida psila Baba & de Saint Laurent, 1996: 494, figs 4d, e, 31. — Baba 2005: 305. MATERIAL EXAMINED. — Wallis and Futuna Islands. MUSORSTOM 7, stn DW 530, 12°32.7’S, 176°39.3’W, 580-600 m, 16. V.1992, 1 ♀ 6.0 mm (MNHN-Ga 5339). — Stn DW 534, 12°23.3’S, 176°42.0’W, 440- 500 m, 16. V.1992, 1 ovig. ♀ 7.9 mm (MNHN-Ga 5340). — Stn DW 540, 12°26.7’S, 177°28.4’W, 600 m, 17. V.1992, 1 juv. 3.8 mm (MNHN-Ga 5341). — Stn DW 571, 12°31,3’S, 176°51.7’W, 502-508 m, 21. V.1992, 1 ovig. ♀ 7.2 mm (MNHN-Ga 5342). — Stn DW 575, 12°30.9’S, 176°52.3’W, 425 m, 21. V.1992, 1 ♂ 7.6 mm (MNHN-Ga 5343). DISTRIBUTION. — Previously known from New Caledonia in 590- 613 m. The new occurrences extend the range to Wallis and Futuna area, in 425- 600 m.Published as part of Macpherson, Enrique & Baba, Keiji, 2006, New species and records of small galatheids (Crustacea, Decapoda, Galatheidae) from the Southwest and Central Pacific Ocean, pp. 443-456 in Zoosystema 28 (2) on page 455, DOI: 10.5281/zenodo.540290

    Onconida modica Baba & de Saint Laurent 1996

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    Onconida modica Baba & de Saint Laurent, 1996 Onconida modica Baba & de Saint Laurent, 1996: 486, figs 27, 33c, d. — Baba 2005: 300. MATERIAL EXAMINED. — Tonga. BORDAU 2, stn CP 1510, 21°04.65’S, 175°22.52’W, 461-497 m, 31.V.2000, 9 ♂♂ 5.7-6.1 mm; 1 ovig. ♀ 5.5 mm; 1 ♀ 5.2 mm (MNHN-Ga 5327). French Polynesia. Austral Archipelago. BENTHAUS, stn DW 1961, 23°20,89’S, 149°33,51’W, 470-800 m, 19.XI.2002, 1 ♂ 5.4 mm (MNHN-Ga 5328). — Stn DW 1983, 23°25.65’S, 150°44.29’W, 300-540 m, 21.XI.2002, 1 ♂ 5.6 mm (MNHN-Ga 5329). — Stn DW 1999, 22°25.12’S, 151°22.15’W, 270-500 m, 23.XI.2002, 3 ovig. ♀♀ 6.0- 6.4 mm; 1 ♀ 5.5 mm (MNHN-Ga 5330). DISTRIBUTION. — Known from Wallis Island and Waterwitch Banc, in 325- 450 m. The present material extends the distribution range to Tonga, in 461-497 m, and French Polynesia (Austral Archipelago), in 270- 800 m.Published as part of Macpherson, Enrique & Baba, Keiji, 2006, New species and records of small galatheids (Crustacea, Decapoda, Galatheidae) from the Southwest and Central Pacific Ocean, pp. 443-456 in Zoosystema 28 (2) on page 455, DOI: 10.5281/zenodo.540290

    Neonida grandis Baba & de Saint Laurent 1996

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    Neonida grandis Baba & de Saint Laurent, 1996 Neonida grandis Baba & de Saint Laurent, 1996: 480, figs 3g, h, 25, 34a. — Baba 2005: 303 (list). MATERIAL EXAMINED. — Solomon Islands. SALOMON 1, stn CP 1831, 10°12.121’S, 161°19.236’W, 135- 325 m, 5.X.2001, 1 ♂ 3.3 mm; 6 ovig. ♀♀ 6.7-7.8 mm (MNHN-Ga 5326). REMARKS This species was only known by the holotype collected in Vanuatu at 397- 402 m. The specimens collected from the Solomon Islands agree quite well with the original description and illustrations provided in Baba & de Saint Laurent (1996). The tubercular processes in the posterior part of the cardiac region are more reduced than in the holotype, being absent in two specimens. This new record extends the distribution of the species to the Solomon Islands. Genus Onconida Baba & de Saint Laurent, 1996Published as part of Macpherson, Enrique & Baba, Keiji, 2006, New species and records of small galatheids (Crustacea, Decapoda, Galatheidae) from the Southwest and Central Pacific Ocean, pp. 443-456 in Zoosystema 28 (2) on pages 454-455, DOI: 10.5281/zenodo.540290

    Magnetic tape: "Answers from Baba Sohan Singh Bhakna to questions about the history and development of the Ghadr Party"

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    Answers from Baba Sohan Singh Bhakna to questions about the history and development of the Ghadr Part

    Uroptychus bispinatus Baba 1988

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    Uroptychus bispinatus Baba, 1988 Figure 38 Uroptychus bispinatus Baba, 1988: 25, fig. 9. — Baba et al. 2009: 40, figs 32-33. — Poore et al. 2011: 328, pl. 6, fig. E. TYPE MATERIAL — Holotype: Indonesia, Molucca Sea between Halmahera and northern Sulawesi, ALBATROSS Stn 5614, 2013 m, female (USNM 150311). [not examined]. MATERIAL EXAMINED — Fiji Islands. BORDAU 1 Stn CP1458, 17°22’S, 179°28’W, 1216-1226 m, 5.III.1999, 3 ♂ 5.3-5.6 mm, 2 ov. ♀ 5.4, 5.8 mm (MNHN-IU-2014-16332). DISTRIBUTION„ Molucca Sea between Halmahera and northern Sulawesi and Taiwan, and now Fiji Islands; 1173- 2013 m. DIAGNOSIS — Carapace as long as broad, greatest breadth 1.6-1.9 × distance between anterolateral spines; unarmed and smooth dorsally (epigastric spines vestigial); lateral margins ridged, with feeble crenulations (in dorsal view) along branchial region; anterolateral spine very small, distinctly posterior to level of small lateral orbital spine or acuminate lateral limit of orbit. Rostrum short triangular, with interior angle of 26-30°, dorsally flattish, length at most one-third that of remaining carapace, breadth less than half carapace breadth measured at posterior carapace margin. Pterygostomian flap anteriorly roundish with very small spine. Excavated sternum with convex anterior margin followed by longitudinal ridge in midline. Sternal plastron slightly broader than long; lateral extremities divergent posteriorly; sternite 3 depressed well, anterior margin deeply excavated in semicircular shape, with submedian spines flanking small median sinus; sternite 4 having anterolateral margins strongly divergent posteriorly, about as long as or slightly shorter than posterolateral margin. Anterolateral margin of sternite 5 convexly strongly divergent posteriorly, as long as anterolateral margin of sternite 4. Abdominal somite 1 without transverse ridge; somite 2 tergite 2.4-2.5 × broader than long; pleural lateral margins barely or slightly concave and posteriorly divergent, ending in bluntly angular tip; pleuron of somite 3 posterolaterally bluntly angular. Telson slightly more than half as long as broad; posterior plate 1.2-1.8 × longer than anterior plate, posterior margin slightly convex or slightly concave, not distinctly emarginate. Eyes relatively broad, 1.4 × longer than broad, distally broadened, proximally narrowed, barely or fully reaching, or slightly overreaching rostral tip. Distal article of antennular peduncle about twice as long as high. Antennal peduncle overreaching apex of rostrum; article 2 without distinct spine; antennal scale varying from slightly overreaching article 4 to terminating in midlength of article 5; distal 2 articles unarmed; breadth of article 5 one-third height of ultimate article of antennule; flagellum of 13-14 segments slightly falling short of distal end of P 1 merus. Mxp1 with bases close to each other, not contiguous. Mxp3 basis with 1 distal denticle on mesial ridge; ischium with flexor margin not rounded distally, crista dentata with 3-7 loosely arranged denticles; merus not flattened, rather thick and unarmed, length 2.5-2.7 × that of ischium. P 1 slender; ischium dorsally with antero-posteriorly compressed, basally broad, short spine; no spine elsewhere; merus 1.0-1.1 × longer than carapace; carpus 1.2-1.4 × longer than merus; palm 3.6-3.7 × (males), 4.4-5.6 × (females) longer than broad, 0.8 × length of carpus; fingers relatively broad distally, spooned on prehensile face, not crossing, length 0.5-0.6 × length of palm. P 2-4 slender; meri with flattish lateral and mesial surfaces, unarmed on dorsal margin, successively shorter posteriorly (P 3 merus 0.9 × length of P 2 merus, P 4 merus 0.9 × length of P 3 merus), subequally broad on P 2-4; P 2 merus 0.8-0.9 × length of carapace, 1.3-1.4 × length of P 2 propodus; P 3 merus 1.1-1.2 × length of P 3 propodus; P 4 merus 0.9-1.1 × length of P 4 propodus; carpi successively slightly shorter posteriorly; carpus-propodus length ratio, 0.7-0.8 on P 2, 0.7 on P 3, 0.6-0.7 on P 4; propodi subequal or successively slightly longer posteriorly; flexor margin inflated at midlength, with 2 or 3 (usually 2) movable spines close to each other and located directly distal to midlength and remote from distal end of article; dactyli much shorter than carpi (dactylus-carpus length ratio, 0.6 on P 2, 0.7 on P 3 and P 4), about half length of propodi (dactylus-propodus length ratio, 0.4 on P 2, 0.4-0.5 on P 3, 0.5 on P 4); relatively slender, flexor margin strongly curving at proximal third, with 2 distal spines of moderate size (ultimate larger) preceded by 8 very small spines oriented parallel to flexor margin, all obscured by setae. Eggs. Number of eggs carried, 8-10; size, 1.60 mm × 1.70 mm - 1.65 × 1.80 mm. Color. A specimen from Taiwan was illustrated in Baba et al. (2009) and Poore et al. (2011). Parasites. One of the males examined bears a rhizocephalan externa. REMARKS — A slight difference between the type and the present material is noted: the excavated sternum bears a central spine on the surface in the type instead of a longitudinal ridge in the present material as well as in the material from Taiwan (Baba et al. 2009). The P 2-4 dactyli bear thick setae along the flexor margin by which the small spines are obscured, as shown in Baba et al. (2009). The presence of these spines was also confirmed in the type material. The small anterolateral spine of the carapace and the P 2-4 dactylar spines oriented parallel to the flexor margin link the species to U. australis (Henderson, 1885) and U. setosipes Baba, 1981 from Japan. Uroptychus bispinatus differs from both in having the pterygostomian flap anteriorly rounded instead of produced, in having the sternite 4 anterolateral margin as long as or slightly shorter than instead of twice as long as the posterolateral margin, in having the P 4 merus 0.9 × instead of 0.6 × as long as the P 3 merus, and in having the P 2-4 propodi with two or three flexor marginal spines remotely distant from the juncture with the dactylus instead of a pair of terminal spines preceded by a row of spines. The species also resembles U. remotispinatus Baba & Tirmizi, 1979 in having a short antennal scale, in having the P 2-4 dactyli with the ultimate spine distinctly larger than the penultimate, and in having the P 2-4 propodi with the distalmost of flexor spines considerably remote from the juncture with the dactyli. Their relationships were discussed by Baba et al. (2009). The coloration was illustrated by Baba et al. (2009) based upon the material from Taiwan.Published as part of Baba, Keiji, 2018, Chirostylidae of the Western and Central Pacific: Uroptychus and a new genus (Crustacea: Decapoda: Anomura), pp. 1-612 in Mémoires du Muséum national d'Histoire naturelle 212 on pages 107-109, DOI: 10.5281/zenodo.376097

    Eumunida bispinata Baba 1990

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    Eumunida bispinata Baba, 1990 Eumunida bispinata Baba, 1990: 925, fig. 1 (Madagascar, 450 m). — Baba, 2005: 209 (synonymies). Eumunida (Eumunidopsis) bispinata. — de Saint Laurent & Poupin, 1996: 373 (no record). Type data: holotype, male, MNHN Ga 1506. Type locality: Madagascar, 12°39.5´S, 48°15.6´E, 450 m.Published as part of Baba, Keiji, Macpherson, Enrique, Poore, Gary C. B., Ahyong, Shane T., Bermudez, Adriana, Cabezas, Patricia, Lin, Chia-Wei, Nizinski, Martha, Rodrigues, Celso & Schnabel, Kareen E., 2008, Catalogue of squat lobsters of the world (Crustacea: Decapoda: Anomura-families Chirostylidae, Galatheidae and Kiwaidae), pp. 1-220 in Zootaxa 1905 (1) on page 16, DOI: 10.11646/zootaxa.1905.1.1, http://zenodo.org/record/513458
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